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用于同时测定妊娠相关血浆蛋白A和人绒毛膜促性腺激素游离β亚基的双标记时间分辨免疫荧光分析法。

Dual-label time-resolved immunofluorometric assay for simultaneous determination of pregnancy-associated plasma protein A and free beta-subunit of human chorionic gonadotrophin.

作者信息

Qin Q, Christiansen M, Lövgren T, Nørgaard-Pedersen B, Pettersson K

机构信息

Department of Biotechnology, University of Turku, Finland.

出版信息

J Immunol Methods. 1997 Jul 14;205(2):169-75. doi: 10.1016/s0022-1759(97)00073-2.

Abstract

Using time-resolved fluorometry, a simple one-step dual-label immunometric assay has been developed, which allows simultaneous determination of pregnancy-associated plasma protein A (PAPP-A) and free beta-subunit of human chorionic gonadotrophin (beta-hCG) in first-trimester maternal serum samples. Two monoclonal antibodies were biotinylated and immobilized onto the surface of streptavidin-coated microtitration plates, and used to capture PAPP-A and beta-hCG. respectively. Europium (Eu) and Samarium (Sm) chelates were conjugated to two additional monoclonal antibodies acting as detection antibodies for PAPP-A and beta-hCG. The assay was performed using a 4-h one-step format. The within-run precision with buffer-based calibrators was below 8% over the working range of PAPP-A (40-10000 mIU/l) and beta-hCG (7.3-525 micrograms/l) and no hook effect was observed. The intra- and inter-assay coefficients of variation were below 7.1% for serum samples. PAPP-A and beta-hCG concentrations measured by the dual assay in 39 first-trimester serum samples correlated excellently with those obtained by DELFIA single-label PAPP-A (r = 0.997) and the beta-hCG part (r = 0.993) of the DELFIA AFP/beta hCG dual-label assay.

摘要

利用时间分辨荧光分析法,开发了一种简单的一步双标记免疫分析方法,该方法可同时测定孕早期孕妇血清样本中的妊娠相关血浆蛋白A(PAPP-A)和人绒毛膜促性腺激素游离β亚基(β-hCG)。将两种单克隆抗体生物素化并固定在链霉亲和素包被的微量滴定板表面,分别用于捕获PAPP-A和β-hCG。铕(Eu)和钐(Sm)螯合物与另外两种单克隆抗体偶联,作为PAPP-A和β-hCG的检测抗体。该分析采用4小时一步法进行。在PAPP-A(40-10000 mIU/l)和β-hCG(7.3-525微克/升)的工作范围内,基于缓冲液的校准品的批内精密度低于8%,未观察到钩状效应。血清样本的批内和批间变异系数低于7.1%。通过双分析测定的39份孕早期血清样本中的PAPP-A和β-hCG浓度与通过DELFIA单标记PAPP-A(r = 0.997)和DELFIA AFP/β hCG双标记分析的β-hCG部分(r = 0.993)获得的浓度高度相关。

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